rs137887044
This is a regulatory region variant variant in the WDR41 gene.
▶GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (1)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Parkinson disease
Rodrigo LM et al. “Imputation and Reanalysis of ExomeChip Data Identifies Novel, Conditional and Joint Genetic Effects on Parkinson's Disease Risk.” Genes 12(5) (2021)
Allele C
OR 1.85
p 2.0e-8
N 10,533
Large GWAS
European
About WDR41
Enables GTPase activator activity. Contributes to guanyl-nucleotide exchange factor activity. Involved in regulation of autophagy. Located in cytoplasm. Part of guanyl-nucleotide exchange factor complex. [provided by Alliance of Genome Resources, Jul 2025]
View all WDR41 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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